A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18071318



Internal ID20638358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:21359501..21360400hg38UCSC Ensembl
chr21:22731821..22732720hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542600
Supporting Variants
Samples
Known GenesNCAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18071318
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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